100542-54-9 Usage
Chemical class
Biphenyl derivatives
Structural features
Presence of two bromine atoms and two methoxy groups on the biphenyl structure
Organic synthesis
Building block for more complex molecules
Chemical research
Used in the study of biphenyl derivatives and related compounds
Pharmaceutical industry
Potential chemical intermediate for the synthesis of biologically active compounds
Coordination chemistry
Acts as a ligand
Material science
Potential application in the development of novel functional materials
Organic electronics
Studied for potential use in organic electronics and optoelectronic devices
Functional groups
Bromine atoms and methoxy groups
Potential uses
a. Synthesis of pharmaceutical compounds
b. Development of new materials with specific properties
c. Enhancement of electronic and optoelectronic device performance
Reactivity
a. Can form coordination complexes with metal ions
b. Can undergo substitution reactions with nucleophiles
c. Can participate in electrophilic aromatic substitution due to the presence of bromine atoms
Stability
Relatively stable under normal conditions, but sensitive to strong nucleophiles or electrophiles
Solubility
Likely soluble in organic solvents such as dichloromethane, acetone, or ethanol
Safety
Handle with care, as it may have potential hazards depending on its reactivity, toxicity, and other properties
Purity
Typically synthesized with high purity for use in research and development
Check Digit Verification of cas no
The CAS Registry Mumber 100542-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,4 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100542-54:
(8*1)+(7*0)+(6*0)+(5*5)+(4*4)+(3*2)+(2*5)+(1*4)=69
69 % 10 = 9
So 100542-54-9 is a valid CAS Registry Number.
100542-54-9Relevant articles and documents
Inhibition of Enterococcus faecalis biofilm formation by highly active lactones and lactams analogues of rubrolides
Pereira, Ulisses A.,Barbosa, Luiz C.A.,Maltha, Célia R.A.,Demuner, Ant?nio J.,Masood, Mohammed A.,Pimenta, Andréa L.
, p. 127 - 138 (2014/06/23)
Seven β-aryl substituted γ-alkylidene-γ-lactones analogues of rubrolides were synthesized from mucobromic acid and converted through a lactamization with isobutylamine into their corresponding γ-hydroxy- γ-lactams (76-85%). These lactams were converted in
